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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5668338insertion1nstd207human GRCh38 chr20: 57,618,042-57,618,042 , GRCh37.p13 chr20: 56,193,098-56,193,098 ZBP1
    nsv5354628translocation1nstd200human GRCh38 chr10: 132,968,643-132,968,643 , GRCh38 chr20: 57,612,376-57,612,376 , GRCh37.p13 chr10: 134,782,147-134,782,147 , GRCh37.p13 chr20: 56,187,432-56,187,432 ZBP1, LINC01168, 1 more genes
    nsv5330051translocation1nstd200human GRCh37 chr10: 134,782,147-134,782,147 , GRCh37 chr20: 56,187,432-56,187,432 , GRCh38.p12 chr10: 132,968,643-132,968,643 , GRCh38.p12 chr20: 57,612,376-57,612,376 ZBP1, LINC01168, 1 more genes
    nsv5286274copy number variation1nstd204human GRCh38.p13 chr20: 57,616,586-57,617,715 , GRCh37.p13 chr20: 56,191,642-56,192,771 ZBP1
    nsv5178950mobile element insertion1nstd203human GRCh38 chr20: 57,609,506-57,609,512 , GRCh37.p13 chr20: 56,184,562-56,184,568 ZBP1
    nsv5174887mobile element insertion1nstd203human GRCh38 chr20: 57,609,501-57,609,512 , GRCh37.p13 chr20: 56,184,557-56,184,568 ZBP1
    nsv5166561mobile element insertion1nstd203human GRCh38 chr20: 57,609,505-57,609,512 , GRCh37.p13 chr20: 56,184,561-56,184,568 ZBP1
    nsv5013341copy number variation1nstd200human GRCh38 chr20: 57,610,776-57,613,719 , GRCh37.p13 chr20: 56,185,832-56,188,775 ZBP1
    nsv4854023copy number variation1nstd200human GRCh37 chr20: 56,185,832-56,188,775 , GRCh38.p12 chr20: 57,610,776-57,613,719 ZBP1
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4500043mobile element insertion1nstd166human GRCh37.p13 chr20: 56,184,557-56,184,557 , GRCh38.p12 chr20: 57,609,501-57,609,501 ZBP1
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4287102copy number variation1nstd166human GRCh37.p13 chr20: 56,189,974-56,204,681 , GRCh38.p12 chr20: 57,614,918-57,629,625 ZBP1
    nsv4277958copy number variation1nstd166human GRCh37.p13 chr20: 56,125,980-56,947,246 , GRCh38.p12 chr20: 57,550,924-58,372,190 , LINC01742, 14 more genes
    nsv4275037copy number variation1nstd166human GRCh37.p13 chr20: 55,859,838-56,531,739 , GRCh38.p12 chr20: 57,284,782-57,956,683 , MTND1P9, 17 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918295copy number variation1nstd102humanPathogenic GRCh38 chr20: 54,594,888-58,190,583 , NCBI36 chr20: 52,644,834-56,199,045 , GRCh37 chr20: 53,211,427-56,765,639 MTRNR2L3, LOC105372687, 59 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912982copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207 ATP5F1E, BMP7, 103 more genes
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